Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 4 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:1990904 | ribonucleoprotein complex | 2 | 3 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: Q4QHK6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 22 |
GO:0003676 | nucleic acid binding | 3 | 22 |
GO:0003723 | RNA binding | 4 | 5 |
GO:0003724 | RNA helicase activity | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 22 |
GO:0004386 | helicase activity | 2 | 22 |
GO:0005488 | binding | 1 | 22 |
GO:0005524 | ATP binding | 5 | 22 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 22 |
GO:0030554 | adenyl nucleotide binding | 5 | 22 |
GO:0032553 | ribonucleotide binding | 3 | 22 |
GO:0032555 | purine ribonucleotide binding | 4 | 22 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 22 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 22 |
GO:0036094 | small molecule binding | 2 | 22 |
GO:0043167 | ion binding | 2 | 22 |
GO:0043168 | anion binding | 3 | 22 |
GO:0097159 | organic cyclic compound binding | 2 | 22 |
GO:0097367 | carbohydrate derivative binding | 2 | 22 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 22 |
GO:0140657 | ATP-dependent activity | 1 | 22 |
GO:1901265 | nucleoside phosphate binding | 3 | 22 |
GO:1901363 | heterocyclic compound binding | 2 | 22 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0003743 | translation initiation factor activity | 4 | 6 |
GO:0008135 | translation factor activity, RNA binding | 3 | 6 |
GO:0045182 | translation regulator activity | 1 | 6 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 115 | 119 | PF00656 | 0.580 |
CLV_C14_Caspase3-7 | 201 | 205 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 23 | 27 | PF00656 | 0.664 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 677 | 679 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 715 | 717 | PF00675 | 0.663 |
CLV_PCSK_FUR_1 | 713 | 717 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.206 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 715 | 717 | PF00082 | 0.635 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.206 |
CLV_PCSK_PC1ET2_1 | 542 | 544 | PF00082 | 0.231 |
CLV_PCSK_PC1ET2_1 | 585 | 587 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 609 | 611 | PF00082 | 0.214 |
CLV_PCSK_PC7_1 | 400 | 406 | PF00082 | 0.202 |
CLV_PCSK_PC7_1 | 711 | 717 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.356 |
DEG_APCC_DBOX_1 | 453 | 461 | PF00400 | 0.448 |
DEG_APCC_DBOX_1 | 514 | 522 | PF00400 | 0.338 |
DEG_APCC_KENBOX_2 | 467 | 471 | PF00400 | 0.464 |
DEG_SCF_FBW7_1 | 651 | 656 | PF00400 | 0.347 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.416 |
DOC_ANK_TNKS_1 | 143 | 150 | PF00023 | 0.508 |
DOC_CKS1_1 | 413 | 418 | PF01111 | 0.492 |
DOC_CKS1_1 | 650 | 655 | PF01111 | 0.335 |
DOC_CKS1_1 | 693 | 698 | PF01111 | 0.589 |
DOC_MAPK_gen_1 | 404 | 413 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 492 | 500 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 542 | 548 | PF00069 | 0.475 |
DOC_MAPK_HePTP_8 | 490 | 502 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 493 | 502 | PF00069 | 0.506 |
DOC_PP1_RVXF_1 | 223 | 230 | PF00149 | 0.421 |
DOC_PP2B_LxvP_1 | 483 | 486 | PF13499 | 0.318 |
DOC_PP2B_LxvP_1 | 567 | 570 | PF13499 | 0.431 |
DOC_PP4_FxxP_1 | 650 | 653 | PF00568 | 0.419 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.259 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.595 |
DOC_USP7_MATH_2 | 22 | 28 | PF00917 | 0.514 |
DOC_USP7_UBL2_3 | 321 | 325 | PF12436 | 0.398 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 649 | 654 | PF00397 | 0.336 |
DOC_WW_Pin1_4 | 692 | 697 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 732 | 737 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.701 |
LIG_14-3-3_CanoR_1 | 12 | 20 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 196 | 203 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 225 | 230 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 364 | 368 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 643 | 653 | PF00244 | 0.544 |
LIG_APCC_ABBA_1 | 40 | 45 | PF00400 | 0.595 |
LIG_APCC_ABBAyCdc20_2 | 617 | 623 | PF00400 | 0.376 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.476 |
LIG_BRCT_BRCA1_1 | 646 | 650 | PF00533 | 0.495 |
LIG_Clathr_ClatBox_1 | 444 | 448 | PF01394 | 0.426 |
LIG_eIF4E_1 | 66 | 72 | PF01652 | 0.632 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.743 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.474 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.594 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.481 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.438 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.600 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.460 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.593 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.567 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.529 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.508 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.488 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.508 |
LIG_FHA_2 | 650 | 656 | PF00498 | 0.446 |
LIG_Integrin_isoDGR_2 | 452 | 454 | PF01839 | 0.205 |
LIG_LIR_Apic_2 | 26 | 32 | PF02991 | 0.655 |
LIG_LIR_Apic_2 | 516 | 522 | PF02991 | 0.270 |
LIG_LIR_Apic_2 | 647 | 653 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 690 | 696 | PF02991 | 0.622 |
LIG_LIR_Gen_1 | 300 | 311 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.649 |
LIG_PCNA_yPIPBox_3 | 313 | 327 | PF02747 | 0.405 |
LIG_PCNA_yPIPBox_3 | 667 | 681 | PF02747 | 0.369 |
LIG_Rb_LxCxE_1 | 201 | 220 | PF01857 | 0.516 |
LIG_Rb_LxCxE_1 | 477 | 496 | PF01857 | 0.322 |
LIG_Rb_pABgroove_1 | 529 | 537 | PF01858 | 0.371 |
LIG_RPA_C_Fungi | 139 | 151 | PF08784 | 0.483 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.353 |
LIG_SH2_CRK | 374 | 378 | PF00017 | 0.351 |
LIG_SH2_CRK | 494 | 498 | PF00017 | 0.340 |
LIG_SH2_CRK | 622 | 626 | PF00017 | 0.346 |
LIG_SH2_NCK_1 | 622 | 626 | PF00017 | 0.292 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.300 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.539 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.219 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.320 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.372 |
LIG_Sin3_3 | 302 | 309 | PF02671 | 0.214 |
LIG_SUMO_SIM_anti_2 | 499 | 505 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 356 | 362 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 365 | 370 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 434 | 439 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 443 | 448 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 496 | 501 | PF11976 | 0.495 |
LIG_TRAF2_1 | 111 | 114 | PF00917 | 0.545 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.646 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.224 |
LIG_TRAF2_1 | 505 | 508 | PF00917 | 0.549 |
LIG_TRAF2_1 | 555 | 558 | PF00917 | 0.244 |
LIG_TYR_ITIM | 301 | 306 | PF00017 | 0.214 |
LIG_UBA3_1 | 305 | 313 | PF00899 | 0.198 |
MOD_CDK_SPxK_1 | 238 | 244 | PF00069 | 0.547 |
MOD_CDK_SPxK_1 | 412 | 418 | PF00069 | 0.334 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.521 |
MOD_CDK_SPxxK_3 | 447 | 454 | PF00069 | 0.224 |
MOD_CDK_SPxxK_3 | 692 | 699 | PF00069 | 0.587 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.702 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.452 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.494 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.323 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.675 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.370 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.416 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.351 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.635 |
MOD_CK1_1 | 732 | 738 | PF00069 | 0.587 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.574 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.529 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.574 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.546 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.373 |
MOD_Cter_Amidation | 713 | 716 | PF01082 | 0.677 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.642 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.656 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.676 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.677 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.437 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.339 |
MOD_GlcNHglycan | 295 | 299 | PF01048 | 0.337 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.224 |
MOD_GlcNHglycan | 34 | 38 | PF01048 | 0.521 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.308 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.461 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.404 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.447 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.595 |
MOD_GlcNHglycan | 639 | 643 | PF01048 | 0.577 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.629 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.790 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.594 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.559 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.723 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.648 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.387 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.277 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.566 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.373 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.473 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.351 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.340 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.338 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.618 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.548 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.583 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.471 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.278 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.682 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.337 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.692 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.462 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.184 |
MOD_PIKK_1 | 633 | 639 | PF00454 | 0.224 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.720 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.509 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.683 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.504 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.292 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.223 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.343 |
MOD_PKA_2 | 633 | 639 | PF00069 | 0.328 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.745 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.599 |
MOD_Plk_1 | 689 | 695 | PF00069 | 0.603 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.413 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.367 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.423 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.382 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.426 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.413 |
MOD_Plk_4 | 646 | 652 | PF00069 | 0.445 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.660 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.636 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.328 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.328 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.470 |
MOD_ProDKin_1 | 649 | 655 | PF00069 | 0.332 |
MOD_ProDKin_1 | 692 | 698 | PF00069 | 0.585 |
MOD_ProDKin_1 | 732 | 738 | PF00069 | 0.688 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.701 |
MOD_SUMO_rev_2 | 612 | 619 | PF00179 | 0.184 |
TRG_DiLeu_BaEn_1 | 380 | 385 | PF01217 | 0.244 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.228 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.259 |
TRG_ER_diArg_1 | 403 | 405 | PF00400 | 0.309 |
TRG_ER_diArg_1 | 559 | 561 | PF00400 | 0.224 |
TRG_ER_diArg_1 | 581 | 584 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 710 | 713 | PF00400 | 0.610 |
TRG_NLS_MonoExtC_3 | 404 | 410 | PF00514 | 0.219 |
TRG_NLS_MonoExtN_4 | 404 | 409 | PF00514 | 0.219 |
TRG_Pf-PMV_PEXEL_1 | 716 | 720 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5R1 | Leptomonas seymouri | 59% | 93% |
A0A1X0NRS9 | Trypanosomatidae | 33% | 95% |
A0A1X0P7J3 | Trypanosomatidae | 23% | 100% |
A0A3Q8ID91 | Leishmania donovani | 28% | 100% |
A0A3Q8IQY6 | Leishmania donovani | 25% | 100% |
A0A3S5H6T7 | Leishmania donovani | 24% | 100% |
A0A3S7WQ33 | Leishmania donovani | 26% | 100% |
A0A3S7WR01 | Leishmania donovani | 91% | 95% |
A0A3S7X9W0 | Leishmania donovani | 26% | 100% |
A0A3S7XAT8 | Leishmania donovani | 23% | 100% |
A2QIL2 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 23% | 91% |
A4H575 | Leishmania braziliensis | 26% | 85% |
A4H5Z5 | Leishmania braziliensis | 69% | 100% |
A4HGR1 | Leishmania braziliensis | 28% | 100% |
A4HK20 | Leishmania braziliensis | 25% | 100% |
A4HK38 | Leishmania braziliensis | 25% | 100% |
A4HP82 | Leishmania braziliensis | 24% | 100% |
A4HTF8 | Leishmania infantum | 27% | 100% |
A4HUC1 | Leishmania infantum | 91% | 95% |
A4HWB0 | Leishmania infantum | 24% | 100% |
A4HZF8 | Leishmania infantum | 22% | 100% |
A4I3T6 | Leishmania infantum | 28% | 100% |
A4IBU1 | Leishmania infantum | 26% | 100% |
A4IDF6 | Leishmania infantum | 23% | 100% |
A4IDI7 | Leishmania infantum | 25% | 100% |
D0A3C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D0A872 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AM86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AN20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9ASV7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9ASZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P0CQ74 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 25% | 100% |
P0CQ75 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 25% | 100% |
Q2UH00 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 24% | 92% |
Q4Q1K8 | Leishmania major | 24% | 100% |
Q4Q1N9 | Leishmania major | 22% | 100% |
Q4Q858 | Leishmania major | 26% | 100% |
Q4QFH1 | Leishmania major | 24% | 100% |
Q4QIG1 | Leishmania major | 27% | 100% |
Q5BCU6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 94% |
Q6CDS6 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 22% | 100% |
V5BII0 | Trypanosoma cruzi | 36% | 100% |